Technology Process of C31H39NO6S
There total 33 articles about C31H39NO6S which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
- Guidance literature:
-
N-propanoyl-(S)-4-benzyl-1,3-oxazolidine-2-thione;
With
titanium tetrachloride;
In
dichloromethane;
at 0 ℃;
for 0.166667h;
Inert atmosphere;
With
(-)-sparteine;
In
dichloromethane;
at 0 ℃;
for 0.333333h;
Inert atmosphere;
C18H24O4;
stereoselective reaction;
Further stages;
DOI:10.1016/j.tet.2012.01.071
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: tetrapropylammonium perruthennate; 4-methylmorpholine N-oxide / dichloromethane / 2 h / 0 - 20 °C / Molecular sieve; Inert atmosphere
2.1: tetrahydrofuran; toluene / 20 h / 90 °C / Inert atmosphere
3.1: dimethylsulfide borane complex / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere
3.2: 0.58 h / 0 - 20 °C
4.1: 1H-imidazole; iodine; triphenylphosphine / benzene / 2 h / 35 °C / Inert atmosphere
5.1: tert.-butyl lithium / diethyl ether; pentane / 0.17 h / -78 °C / Inert atmosphere
6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 4 h / 45 °C / Inert atmosphere
7.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere
8.1: titanium tetrachloride / dichloromethane / 0.17 h / 0 °C / Inert atmosphere
8.2: 0.33 h / 0 °C / Inert atmosphere
With
1H-imidazole; tetrapropylammonium perruthennate; dimethylsulfide borane complex; tetrabutyl ammonium fluoride; iodine; tert.-butyl lithium; sulfur trioxide pyridine complex; titanium tetrachloride; dimethyl sulfoxide; 4-methylmorpholine N-oxide; triethylamine; triphenylphosphine;
In
tetrahydrofuran; diethyl ether; dichloromethane; toluene; pentane; benzene;
7.1: Parikh-Doering oxidation;
DOI:10.1016/j.tet.2012.01.071
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: tert.-butyl lithium / diethyl ether; pentane / 0.17 h / -78 °C / Inert atmosphere
2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 4 h / 45 °C / Inert atmosphere
3.1: sulfur trioxide pyridine complex; dimethyl sulfoxide; triethylamine / dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere
4.1: titanium tetrachloride / dichloromethane / 0.17 h / 0 °C / Inert atmosphere
4.2: 0.33 h / 0 °C / Inert atmosphere
With
tetrabutyl ammonium fluoride; tert.-butyl lithium; sulfur trioxide pyridine complex; titanium tetrachloride; dimethyl sulfoxide; triethylamine;
In
tetrahydrofuran; diethyl ether; dichloromethane; pentane;
3.1: Parikh-Doering oxidation;
DOI:10.1016/j.tet.2012.01.071